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Associate Director of Clinical Medical Writing
2 months ago
BioMarin is seeking an experienced Associate Director of Clinical Medical Writing to join our team. As a key member of our Development Sciences department, you will be responsible for overseeing the medical writing function and ensuring the development of high-quality documents that support our corporate goals and objectives.
Key Responsibilities- Lead a team of medical writers in the development of clinical and regulatory documents, including protocols, informed consent forms, and clinical study reports.
- Collaborate with cross-functional teams to ensure timely and accurate delivery of documents.
- Develop and implement processes and templates to improve efficiency and consistency in medical writing.
- Manage vendor relationships and oversee the development of outsourced projects.
- Provide training and mentorship to junior medical writers to ensure their growth and development.
- Minimum of 10 years of experience as a medical writer in the pharmaceutical industry.
- At least 3 years of experience in a leadership role, managing a team of medical writers.
- Advanced understanding of the drug development process, biostatistical and clinical research concepts, and clinical study conduct.
- Excellent communication and project management skills.
BioMarin offers a dynamic and collaborative work environment, competitive compensation and benefits package, and opportunities for professional growth and development.
